A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758086



Internal ID20533946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107730124..107730124hg38UCSC Ensembl
chr7:107370569..107370569hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381551
hg191551
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758086
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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